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Title 21 - Food and Drugs
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CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
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SUBCHAPTER A—GENERAL (parts 1 to 99)
CFR
Title 1 - General Provisions
Title 2 - Grants and Agreements
Title 3 - The President
Title 4 - Accounts
Title 5 - Administrative Personnel
Title 6 - Domestic Security
Title 7 - Agriculture
Title 8 - Aliens and Nationality
Title 9 - Animals and Animal Products
Title 10 - Energy
Title 11 - Federal Elections
Title 12 - Banks and Banking
Title 13 - Business Credit and Assistance
Title 14 - Aeronautics and Space
Title 15 - Commerce and Foreign Trade
Title 16 - Commercial Practices
Title 17 - Commodity and Securities Exchanges
Title 18 - Conservation of Power and Water Resources
Title 19 - Customs Duties
Title 20 - Employees' Benefits
Title 21 - Food and Drugs
Title 22 - Foreign Relations
Title 23 - Highways
Title 24 - Housing and Urban Development
Title 25 - Indians
Title 26 - Internal Revenue
Title 27 - Alcohol, Tobacco Products and Firearms
Title 28 - Judicial Administration
Title 29 - Labor
Title 30 - Mineral Resources
Title 31 - Money and Finance: Treasury
Title 32 - National Defense
Title 33 - Navigation and Navigable Waters
Title 34 - Education
Title 35 - Panama Canal
Title 36 - Parks, Forests, and Public Property
Title 37 - Patents, Trademarks, and Copyrights
Title 38 - Pensions, Bonuses, and Veterans' Relief
Title 39 - Postal Service
Title 40 - Protection of Environment
Title 41 - Public Contracts and Property Management
Title 42 - Public Health
Title 43 - Public Lands: Interior
Title 44 - Emergency Management and Assistance
Title 45 - Public Welfare
Title 46 - Shipping
Title 47 - Telecommunication
Title 48 - Federal Acquisition Regulations System
Title 49 - Transportation
Title 50 - Wildlife and Fisheries
SUBCHAPTER A—GENERAL (parts 1 to 99)
PART 1—GENERAL ENFORCEMENT REGULATIONS
PART 2—GENERAL ADMINISTRATIVE RULINGS AND DECISIONS
PART 3—PRODUCT JURISDICTION
PART 5—ORGANIZATION
PART 7—ENFORCEMENT POLICY
PART 10—ADMINISTRATIVE PRACTICES AND PROCEDURES
PART 11—ELECTRONIC RECORDS; ELECTRONIC SIGNATURES
PART 12—FORMAL EVIDENTIARY PUBLIC HEARING
PART 13—PUBLIC HEARING BEFORE A PUBLIC BOARD OF INQUIRY
PART 14—PUBLIC HEARING BEFORE A PUBLIC ADVISORY COMMITTEE
PART 15—PUBLIC HEARING BEFORE THE COMMISSIONER
PART 16—REGULATORY HEARING BEFORE THE FOOD AND DRUG ADMINISTRATION
PART 17—CIVIL MONEY PENALTIES HEARINGS
PART 19—STANDARDS OF CONDUCT AND CONFLICTS OF INTEREST
PART 20—PUBLIC INFORMATION
PART 21—PROTECTION OF PRIVACY
PART 25—ENVIRONMENTAL IMPACT CONSIDERATIONS
PART 26—MUTUAL RECOGNITION OF PHARMACEUTICAL GOOD MANUFACTURING PRACTICE REPORTS, MEDICAL DEVICE QUALITY SYSTEM AUDIT REPORTS, AND CERTAIN MEDICAL DEVICE PRODUCT EVALUATION REPORTS: UNITED STAT
PART 50—PROTECTION OF HUMAN SUBJECTS
PART 54—FINANCIAL DISCLOSURE BY CLINICAL INVESTIGATORS
PART 56—INSTITUTIONAL REVIEW BOARDS
PART 58—GOOD LABORATORY PRACTICE FOR NONCLINICAL LABORATORY STUDIES
PART 60—PATENT TERM RESTORATION
PART 70—COLOR ADDITIVES
PART 71—COLOR ADDITIVE PETITIONS
PART 73—LISTING OF COLOR ADDITIVES EXEMPT FROM CERTIFICATION
PART 74—LISTING OF COLOR ADDITIVES SUBJECT TO CERTIFICATION
PART 80—COLOR ADDITIVE CERTIFICATION
PART 81—GENERAL SPECIFICATIONS AND GENERAL RESTRICTIONS FOR PROVISIONAL COLOR ADDITIVES FOR USE IN FOODS, DRUGS, AND COSMETICS
PART 82—LISTING OF CERTIFIED PROVISIONALLY LISTED COLORS AND SPECIFICATIONS
PART 99—DISSEMINATION OF INFORMATION ON UNAPPROVED/NEW USES FOR MARKETED DRUGS, BIOLOGICS, AND DEVICES
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